LABELS · 5b2d0f4e-5bba-4048-a2f0-bcb4b779efc0
Verzenio
Open original source → · Download preserved record
Preserved label snapshot, not confirmation of a current approved indication. Approval/withdrawal status must be checked for the exact disease, setting and regimen.
- Label effective date
- 2026-07-13
- Captured
- 2026-09-09T23:37:47.659725+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source text
- 1 INDICATIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. ( 1.1 , 14.1 ) in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. ( 1.2 ) in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. ( 1.2 ) as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting. ( 1.2 ) 1.1 Early Breast Cancer VERZENIO ® (abemaciclib) is indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence [see Clinical Studies ( 14.1 )]. 1.2 Advanced or Metastatic Breast Cancer VERZENIO (abemaciclib) is indicated: in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting.
Full extracted label fields
- application numbers
- NDA208716
- boxed warning exact
- brand names
- Verzenio
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=be4bc0de-0fdc-4d46-8d25-be43c79e6a06
- generic names
- ABEMACICLIB
- id
- 5b2d0f4e-5bba-4048-a2f0-bcb4b779efc0
- indications and usage exact
- 1 INDICATIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. ( 1.1 , 14.1 ) in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. ( 1.2 ) in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. ( 1.2 ) as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting. ( 1.2 ) 1.1 Early Breast Cancer VERZENIO ® (abemaciclib) is indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence [see Clinical Studies ( 14.1 )]. 1.2 Advanced or Metastatic Breast Cancer VERZENIO (abemaciclib) is indicated: in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting.
- indications and usage tables exact
- is original packager
- true
- manufacturer names
- Eli Lilly and Company
- matched search terms
- cancer
- package ndcs
- 0002-4483-54
- 0002-4483-62
- 0002-4815-54
- 0002-4815-62
- 0002-5337-54
- 0002-5337-63
- 0002-5337-62
- 0002-6216-54
- product ndcs
- 0002-4483
- 0002-4815
- 0002-5337
- 0002-6216
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- record type
- complete_spl_indications_section_candidate
- routes
- ORAL
- rxcuis
- 1946830
- 1946836
- 1946838
- 1946840
- 1946842
- 1946844
- 1946846
- 1946848
- source batch
- file
- /private/tmp/cancer-full-research/indications/raw/labels-00300.json
- meta
- disclaimer
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.
- last updated
- 2026-09-09
- results
- limit
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- skip
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- total
- 830
- sha256
- bbaf8e3e49a06d91fa717d034adb1798932735c99e42d8d769cf5f9eb31d345e
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%225b2d0f4e-5bba-4048-a2f0-bcb4b779efc0%22
- spl effective date
- 2026-07-13
- spl effective time
- 20260713
- spl set id
- be4bc0de-0fdc-4d46-8d25-be43c79e6a06
- spl version
- 30
- substance names
- ABEMACICLIB
- uniis
- 60UAB198HK
- verification flags
- oncology_keyword_candidate_not_clinically_classified
- spl_text_not_verified_identical_to_latest_approved_label
- individual_indications_not_split_or_reconciled
- fda_label_posted_after_spl_effective_date_requires_version_review
Drugs@FDA application source records
- application number
- NDA208716
- payload
- all indexed label documents
- Appl No
- 208716
- Application Docs Date
- 2017-09-28 00:00:00
- Application Docs ID
- 49872
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2017/208716Orig1s000lbl.pdf
- Submission No
- 1
- Submission Type
- ORIG
- Appl No
- 208716
- Application Docs Date
- 2018-08-21 00:00:00
- Application Docs ID
- 55257
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2018/208716s001lbl.pdf
- Submission No
- 1
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2019-09-11 00:00:00
- Application Docs ID
- 59972
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2019/208716s003lbl.pdf
- Submission No
- 3
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2020-03-31 00:00:00
- Application Docs ID
- 62394
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2020/208716s004lbl.pdf
- Submission No
- 4
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2021-10-13 00:00:00
- Application Docs ID
- 68965
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/208716s006s007s008lbl.pdf
- Submission No
- 6
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2021-10-13 00:00:00
- Application Docs ID
- 68966
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/208716s006s007s008lbl.pdf
- Submission No
- 7
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2021-10-13 00:00:00
- Application Docs ID
- 68967
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/208716s006s007s008lbl.pdf
- Submission No
- 8
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2023-03-03 00:00:00
- Application Docs ID
- 73673
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2023/208716s010s011lbl.pdf
- Submission No
- 11
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2023-03-03 00:00:00
- Application Docs ID
- 73674
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2023/208716s010s011lbl.pdf
- Submission No
- 10
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2024-11-14 00:00:00
- Application Docs ID
- 80213
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2024/208716s017lbl.pdf
- Submission No
- 17
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2025-03-03 00:00:00
- Application Docs ID
- 81385
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2025/208716s019lbl.pdf
- Submission No
- 19
- Submission Type
- SUPPL
- Appl No
- 208716
- Application Docs Date
- 2026-07-15 00:00:00
- Application Docs ID
- 86561
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/208716s021lbl.pdf
- Submission No
- 21
- Submission Type
- SUPPL
- all submission records
- Appl No
- 208716
- Review Priority
- PRIORITY
- Submission Class Code ID
- 7
- Submission No
- 1
- Submission Status
- AP
- Submission Status Date
- 2017-09-28 00:00:00
- Submission Type
- ORIG
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 1
- Submission Status
- AP
- Submission Status Date
- 2018-08-17 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- 901 REQUIRED
- Submission Class Code ID
- 3
- Submission No
- 3
- Submission Status
- AP
- Submission Status Date
- 2019-09-09 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 4
- Submission Status
- AP
- Submission Status Date
- 2020-03-30 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 6
- Submission Status
- AP
- Submission Status Date
- 2021-10-12 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 7
- Submission Status
- AP
- Submission Status Date
- 2021-10-12 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 8
- Submission Status
- AP
- Submission Status Date
- 2021-10-12 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 10
- Submission Status
- AP
- Submission Status Date
- 2023-03-03 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 11
- Submission Status
- AP
- Submission Status Date
- 2023-03-03 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 17
- Submission Status
- AP
- Submission Status Date
- 2024-11-13 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 19
- Submission Status
- AP
- Submission Status Date
- 2025-02-27 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 208716
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 21
- Submission Status
- AP
- Submission Status Date
- 2026-07-13 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- application number
- NDA208716
- approval interpretation
- Application linkage and approved submission are not indication-level current approval verification
- current indication status
- not_reconciled
- drugsfda url
- https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=208716
- has approved submission record
- true
- latest approved submission date
- 2026-07-13
- latest label selection rule
- max FDA ApplicationDocsDate, including all ties; posting date is not approval date and latest indexed document may be incomplete
- latest posted label documents
- Appl No
- 208716
- Application Docs Date
- 2026-07-15 00:00:00
- Application Docs ID
- 86561
- Application Docs Title
- 0
- Application Docs Type ID
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- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/208716s021lbl.pdf
- Submission No
- 21
- Submission Type
- SUPPL
- official application record
- Appl No
- 208716
- Appl Public Notes
- Appl Type
- NDA
- Sponsor Name
- ELI LILLY AND CO
- openfda application present
- true
- products
- Active Ingredient
- ABEMACICLIB
- Appl No
- 208716
- Drug Name
- VERZENIO
- Form
- TABLET;ORAL
- Product No
- 001
- Reference Drug
- 1
- Reference Standard
- 0
- Strength
- 50MG
- marketing status
- Prescription
- Active Ingredient
- ABEMACICLIB
- Appl No
- 208716
- Drug Name
- VERZENIO
- Form
- TABLET;ORAL
- Product No
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- Reference Drug
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- Reference Standard
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- Strength
- 100MG
- marketing status
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- Active Ingredient
- ABEMACICLIB
- Appl No
- 208716
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- VERZENIO
- Form
- TABLET;ORAL
- Product No
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- Reference Drug
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- Reference Standard
- 0
- Strength
- 150MG
- marketing status
- Prescription
- Active Ingredient
- ABEMACICLIB
- Appl No
- 208716
- Drug Name
- VERZENIO
- Form
- TABLET;ORAL
- Product No
- 004
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- 200MG
- marketing status
- Prescription
Source passages and status connections
Passage 1 · positive indication candidate
- application numbers
- NDA208716
- brand names
- Verzenio
- classification reasons
- explicit_positive_indication_predicate
- tumor_or_malignant_hematology_words_in_positive_statement
- positive_statement_also_contains_qualification_review_required
- clinical review status
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- 1 INDICATIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. ( 1.1 , 14.1 ) in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor rec
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- 1 INDICATIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence.
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- structured fields status
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- Source null
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Passage 2 · positive indication candidate
- application numbers
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- Verzenio
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- the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. ( 1.1 , 14.1 ) in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. ( 1.2 ) in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast
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Triangle